5-Octyloxy-2-(3-fluorophenyl)pyrimidine → 5-Octyloxy-2-[4-(3-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)-3-fluorophenyl]pyrimidine
반응식
[CH2:1]([O:9][C:10]1[CH:11]=[N:12][C:13]([C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([F:22])[CH:17]=2)=[N:14][CH:15]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].C(OC1C=NC(C2C=CC([O:42][CH2:43][CH2:44][CH2:45][O:46][CH2:47][C:48]([O:51][C:52]([F:62])([F:61])[C:53]([F:60])([F:59])[O:54][C:55]([F:58])([F:57])[F:56])([F:50])[F:49])=CC=2)=NC=1)CCCCC>>[CH2:1]([O:9][C:10]1[CH:15]=[N:14][C:13]([C:16]2[CH:21]=[CH:20][C:19]([O:42][CH2:43][CH2:44][CH2:45][O:46][CH2:47][C:48]([O:51][C:52]([F:61])([F:62])[C:53]([F:59])([F:60])[O:54][C:55]([F:57])([F:58])[F:56])([F:50])[F:49])=[C:18]([F:22])[CH:17]=2)=[N:12][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]참가 물질
3
반응물 2
생성물 1
실험 절차
The title compound was prepared essentially as in Example 1 by combining 5-octyloxy-2-(3-fluorophenyl)pyrimidine (2.0 g, 6.3 mmol) with 3-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy chloride (2.5 g, 7.0 mmol, Example 17). The reaction mixture was quenched with water, and the resulting crude product was further purified by recrystallization from ethanol, followed by Kugelrohr distillation (210-18° C. at 0.15 torr), to provide a yield of 3.2 g.